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Exercise Physiology in Patients With Aortic Aneurysm and Its Correlation With Mechanical Properties of Aortic Tissue

Exercise Physiology in Patients With Aortic Aneurysm and Its Correlation With Mechanical Properties of Aortic Tissue

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06789809
Enrollment
35
Registered
2025-01-23
Start date
2023-11-23
Completion date
2029-03-31
Last updated
2026-01-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aortic Aneurysm

Brief summary

Aortic aneurysm patients benefit from exercise yet patients and physicians do not know a safe level. Cardiac MRI (CMR) is the most comprehensive imaging modality for phenotypic evaluation of patients with cardiac disease but it has not been used to study aneurysm patients. The purpose of this project is use exercise CMR to understand regional aortic function and quantify aortic elasticity in these populations while exercising. This project will correlate the exercise CMR data with the biomechanical properties of the patient's aortic tissue, including epiaortic ultrasound and TEE performed during aortic repair, and explanted aortic specimens subjected to ex vivo uniaxial tensile testing. Correlating this data with aortic response to exercise will allow us to understand how aortic size, in vivo circumferential strain values, ex vivo aortic efficiency and mechanical failure all relate to exercise physiology.

Detailed description

Engaging in regular exercise in controls lowers blood pressure over time, and this is associated with a lower risk of future aortic complications. However, it is not known what level of exercise is safe for aneurysm patients. Cardiac MRI (CMR) is the most comprehensive imaging modality for phenotypic evaluation of patients with cardiac disease. It has been limited in its use because exercise stress MRI is not widely available due to the need for MRI safe exercise equipment. However, the Cleveland Clinic has purchased a Lode MRI compatible exercise ergometer that is FDA approved and compatible with our 3T cardiac MRI scanner. By conducting a study using this imaging modality we will be able to observe aortic blood flow, specifically compliance, distensibility, maximum rates of systolic distension and diastolic recoil, at different locations along the ascending and descending aorta, as well as aortic pulse wave velocity. A more comprehensive analysis of these variables will be critical to understanding how the aorta responds during times of stress in aneurysm patients.

Interventions

DIAGNOSTIC_TESTExercise MRI

Exercise stress MRI with ergometer

Sponsors

The Cleveland Clinic
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Healthy controls for baseline comparison 1. Must be 18 years or older 2. No history of cardiovascular disease, neither hypertension, diabetes nor hypercholesterolemia 2. Aneurysm patients who have not yet been operated on but are currently being monitored 1. Must be 18 years or older 2. No history of operation for aortic aneurysm 3. Pre-operative aneurysm patients: imaged pre-operatively and 12 months 1. Patients admitted at the CCF cardiothoracic services for elective surgery due to aortic aneurysms 2. Must be 18 years or older

Exclusion criteria

For all patients: * Contra-indication for MRI * Heart pacemaker/defibrillator. * Electronic/implanted stimulators or devices, including deep brain stimulator, vagus nerve stimulator, bladder stimulator, spine stimulator, neurostimulators; implanted electrodes or wires. * Cochlear implant or other ear implants. * Implanted drug pumps (insulin, narcotic/pain medications, drugs to treat spasticity). * Programmable shunt. * Aneurysm clips and coils. * Stents (not located in heart). * Filters (for example, blood clot filters). * Metal fragment in your body or eye (eg, BBs, bullets, shrapnel, metal pieces or shavings). * Congenital heart diseases such as patent ductus arteriosus, coarctation of aorta, ASD and VSD * Presence of A-V fistula or intracardiac shunts * Moderate or severe dysfunction in multiple valves * Patients with significant claustrophobia * Patients unable to pedal a supine bicycle * Those who require supplemental oxygen Specific

Design outcomes

Primary

MeasureTime frameDescription
Arterial Complianceup to 12 monthsAbsolute change in arterial volume for a change in pressure

Countries

United States

Contacts

Primary ContactJonathan Putnam
putnamj2@ccf.org740-701-8226

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026